ZipRecruiter

Log In

1

Esource Jobs (NOW HIRING)

Crio, Inc.

Sponsor Project Manager

CRIO's eSource and CTMS system is a leading, modern, enterprise platform built for clinical research sites. Since CRIO's launch in 2016, CRIO has established the leading brand position in eSource and ...

Gastromed, LLC

Sub-Investigator (Nurse Practitioner)

Miami, FL · On-site

$98K - $133K/yr

Maintain accurate, timely, and complete documentation in the eSource systems MINIMUM QUALIFICATIONS * Licensed Nurse Practitioner in the state of Florida (active and in good standing) * Minimum 1-2 ...

Clinical Ink

Software Testing Manager

Winston Salem, NC · On-site

Company Description Founded in 2007, Clinical Ink is an innovation-driven eSource solutions company committed to making clinical research easier for sites, sponsors, subjects and regulators. Guided ...

Clinical Ink

Data Management Intern

Horsham, PA

Company Description Founded in 2007, Clinical Ink is an innovation-driven eSource solutions company committed to making clinical research easier for sites, sponsors, subjects and regulators. Guided ...

Clinical Ink

Data Management Intern

Horsham, PA · On-site

Company Description Founded in 2007, Clinical Ink is an innovation-driven eSource solutions company committed to making clinical research easier for sites, sponsors, subjects and regulators. Guided ...

QPS, LLC

Site Systems Coordinator

Springfield, MO · On-site

This role ensures that ClinSpark (eSource) builds are aligned with real-world site workflows prior to team structured review, reducing operational burden while maintaining clear build ownership and ...

Crio, Inc.

Community Engagement Specialist

$60K - $72K/yr

CRIO is a leading provider of eSource solutions for clinical research. Our platform streamlines clinical data collection and management, ensuring protocol compliance and reducing errors. By ...

next page

Showing results 1-20

All JobsEsource Jobs

Esource information

See salary details

$8

$26

$61

How much do esource jobs pay per hour?

As of Jun 16, 2026, the average hourly pay for esource in the United States is $26.34, according to ZipRecruiter salary data. Most workers in this role earn between $15.14 and $30.77 per hour, depending on experience, location, and employer.

What are the main responsibilities of an Esource Specialist in a clinical research setting?

As an Esource Specialist, your primary responsibilities include implementing and maintaining electronic source data systems for clinical studies, ensuring data accuracy, and supporting compliance with regulatory standards. You will often work closely with clinical research coordinators, data managers, and IT teams to set up, test, and troubleshoot eSource platforms. Additionally, you may assist in training site staff, creating documentation, and participating in data quality audits. This role is a key part of the clinical research process, helping streamline workflows and contribute to the reliability of study outcomes.

What is an Esource job?

An Esource job typically involves managing electronic source data in clinical research or healthcare settings. Professionals in this role ensure the accurate collection, storage, and integration of digital records, often replacing traditional paper documentation. They may work with electronic data capture (EDC) systems, regulatory compliance, and data quality control. Strong attention to detail and familiarity with clinical or regulatory environments are essential.

What are the key skills and qualifications needed to thrive in the Esource position, and why are they important?

To succeed as an Esource Specialist, you need a background in clinical research, an understanding of data management, and familiarity with regulatory guidelines, often supported by a degree in life sciences or a related field. Expertise in electronic data capture (EDC) systems, eSource platforms such as Medidata Rave or OpenClinica, and possibly certifications in clinical data management are highly valued. Attention to detail, problem-solving ability, and strong collaboration skills are essential for working with research teams and ensuring data integrity. These competencies are vital to ensure accurate, compliant, and efficient collection and management of clinical trial data.

More about Esource jobs
What states have the most Esource jobs? States with the most job openings for Esource jobs include:
What job categories do people searching Esource jobs look for? The top searched job categories for Esource jobs are:
Esource jobs near you
Infographic showing various Esource job openings in the United States as of June 2026, with employment types broken down into 75% Full Time, and 25% Part Time. Highlights an 100% In-person job distribution, with an average salary of $54,791 per year, or $26.3 per hour.

ECOA Study Build Programmer

2T Consulting

Indianapolis, IN • On-site

Full-time

Posted 6 days ago

Job description

Role Summary

We are seeking an eCOA Study Build Programmer to design, configure, program, and test electronic Clinical Outcome Assessment (eCOA) and clinical data collection systems. The role ensures accurate study build execution, data mapping, and compliance with clinical protocol requirements while supporting end-to-end clinical trial data acquisition and reporting needs.

Key Responsibilities
  • Gather and interpret eCOA design specifications to support clinical trial implementation
  • Design, program, and test eCOA/eDC/eSource data collection systems and study databases
  • Build and validate eCRF screens, including data entry workflows and edit checks
  • Implement data repository mappings aligned with clinical data standards and study protocols
  • Ensure accurate data flow from patient data capture to analysis datasets
  • Collaborate with Clinical Build Programmers to deliver complete study builds
  • Analyze clinical protocols and translate requirements into system specifications
  • Support study-level deliverables including Data Management Plans, database setup, and study documentation
  • Execute post-production changes and assess impact on study design and data integrity
  • Support submission, inspection, and regulatory response activities
  • Contribute to cross-functional or high-complexity study/program implementations
Required Skills & Qualifications
  • Strong experience in Clinical Domain (eCOA, eDC, eSource, or Direct Data Capture)
  • Proficiency in JavaScript, JSON, HTML, SpEL expressions, and C#
  • Experience designing and building electronic CRF (eCRF) screens with validations
  • Strong understanding of clinical protocols and clinical terminology interpretation
  • Experience in clinical data systems, testing, and validation workflows
  • Knowledge of clinical data standards and data mapping concepts
  • Ability to analyze data flow from capture to analysis and reporting
Preferred Skills
  • Experience in clinical data analytics and visualization
  • Exposure to clinical data warehouse or data repository systems
  • Understanding of clinical trial regulatory and submission processes
  • Experience working in cross-functional clinical study teams

Apply